- Bristol Myers Squibb (Cambridge, MA)
- …internal and external networks **Position Responsibilities** **Medical Monitoring** + Independent medical monitor for clinical trials from Phase 1 through ... primary source of medical accountability and oversight for multiple clinical trials + Manages Phase I/II studies,...oversight for multiple clinical trials + Manages Phase I/II studies, with demonstrated decision making capabilities +… more
- IQVIA (Durham, NC)
- **Job Level:** FSP Senior or Principal Biostatistician for Early Phase Clinical Development (PK) **Location:** Home-based in the US or Canada **Why DSSS?** Data ... to study synopses and protocols. + Write the statistical sections of clinical trial protocols, including sample size calculations, while consulting with internal and… more
- IQVIA (Durham, NC)
- …field with 7+ years of industry experience. + **At least 3 years in Phase 2/3 clinical trial experience.** + Demonstrated ability to work pro-actively and ... **Job Level: FSP Principal Biostatistician, Late Phase ** **Location:** Home-based in the US or Canada **Why DSSS?** Data Sciences Staffing Solutions, DSSS, is a unit… more
- IQVIA (Durham, NC)
- **Job Level: FSP** Principal Biostatistician (FSP) for Early Phase **Location:** Home-based in the US or Canada **Why DSSS?** Data Sciences Staffing Solutions, DSSS ... statistical input to study protocols. + Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts. + Write… more
- Lilly (Stamford, CT)
- …as needed to inform development and manage issues. For preclinical and early clinical development programs, the GRL leads the US and Canada submissions and agency ... documents by leveraging team expertise, as well as scientific, drug/device clinical development and knowledge from health authorities such as regulatory policies,… more
- Astellas Pharma (Denver, CO)
- …assigned sites for specific trials. Trials may include both early and late phase clinical trials. + Develops meaningful site relationships through consistent ... our website at www.astellas.com . **Purpose and Scope:** A Clinical Site Monitor serves as the primary...with study team for the activities during site activation phase to speed up the process and activate the… more
- Edwards Lifesciences (Pittsburgh, PA)
- …subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good ... our inspiring journey. We are searching for a **Senior** ** Clinical Research Monitor ** to join Edwards Transcatheter...finalization + Experience with a variety of study phases ( Phase I-IV) including complex trials, in pharmaceutical or medical… more
- Texas A&M University - Faculty (Houston, TX)
- …Practice, Education, & Research) to ensure a comprehensive and effective clinical skills program. Curriculum Integration: Partner with Phase Assistant ... Feedback: Provide feedback on student performance to academic success and Phase Deans, facilitating continuous quality improvement of clinical curricula… more
- WuXi AppTec (Austin, TX)
- …and within budget. The Senior CRA will work to manage, oversee and may monitor /co- monitor clinical trial sites. **Essential Job Functions:** + Participate in ... Organization (CRO) providing a comprehensive range of services in clinical development. We provide Phase I to...project needs + Approximately 50% to study sites to monitor , co- monitor , train, attend Investigator meetings or… more
- University of Pennsylvania (Philadelphia, PA)
- …supports a diverse group of investigators, involving work on a wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated, ... of investigators, involving work on a wide spectrum of clinical trials ranging from phase I to...patient visits and any necessary testing. Conduct patient visits. Monitor patients per protocol requirements and ensure adherence to… more